@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_head {
  this: np:hasAssertion dgn-np:NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_assertion ;
    np:hasProvenance dgn-np:NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_provenance ;
    np:hasPublicationInfo dgn-np:NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_assertion a np:Assertion .
  dgn-np:NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_provenance a np:Provenance .
  dgn-np:NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_assertion {
  miriam-gene:999 a ncit:C16612 .
  lld:C0036631 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_provenance {
  dgn-np:NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_assertion dcterms:description "[Occurrence of structural genetic alterations was analyzed in 18 seminomas and 22 non-seminomas for genes involved in the malignant tumour phenotype: cadherin 1, Type 1, E-cadherin (Epithelial), CDH1; adenomatous polyposis coli, APC; NME/NM23 nucleoside diphosphate kinase 1, NME1; tumour protein P53, TP53; cyclin-dependent kinase inhibitor 2A, CDKN2A; retinoblastoma 1, RB1; RAD51 recombinase, RAD51; mutS homolog 2, MSH2; MutL homolog 1, MLH1; breast cancer 1, early onset, BRCA1; BCL2-Associated X Protein, BAX; ATP-Binding Cassette, Sub-Family G (WHITE), Member 2, ABCG2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
    sio:SIO_000772 miriam-pubmed:25075023 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
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  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^xsd:date .
  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:32+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetv3.0rdf ;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v3.0.0.0" .
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}